Votava-Smith Jodie K, Pitukcheewanont Pisit, Randolph Linda M, Chmait Ramen H
Division of Cardiology, Children's Hospital Los Angeles, Los Angeles, Calif., USA.
Fetal Diagn Ther. 2017;41(3):234-236. doi: 10.1159/000444852. Epub 2016 Mar 17.
Recipients of the twin-twin transfusion syndrome (TTTS) often develop cardiac manifestations, but arterial calcification has rarely been reported. Generalized arterial calcification of infancy (GACI) is a genetic disorder with high infantile mortality. We report the case of a TTTS recipient with moderate cardiomyopathy at diagnosis who developed progressive calcification of the pulmonary arteries and aorta after successful in utero laser therapy. Postnatally, both twins were diagnosed with a heterozygous ABCC6 gene mutation associated with GACI. The recipient had progressive supravalvular pulmonary and aortic stenosis, was treated with bisphosphonate therapy, and successfully underwent cardiac surgery at 4 months of age. The donor twin with the same mutation remained phenotypically normal at 15 months of age. This case illustrates monozygotic fetuses with discordant in utero hemodynamics, with subsequent development of phenotypic differences. TTTS recipients with arterial calcifications should undergo genetic testing for GACI.
双胎输血综合征(TTTS)的受血儿常出现心脏表现,但动脉钙化鲜有报道。婴儿期全身性动脉钙化(GACI)是一种遗传性疾病,婴儿死亡率很高。我们报告了一例TTTS受血儿,诊断时患有中度心肌病,在子宫内激光治疗成功后出现肺动脉和主动脉的进行性钙化。出生后,双胞胎均被诊断出与GACI相关的ABCC6基因杂合突变。受血儿患有进行性肺动脉瓣上和主动脉瓣上狭窄,接受了双膦酸盐治疗,并在4个月大时成功接受了心脏手术。具有相同突变的供血儿在15个月大时表型仍正常。该病例说明了单卵胎儿在子宫内血流动力学不一致,随后出现表型差异。有动脉钙化的TTTS受血儿应接受GACI的基因检测。